CN1225489C - 可光致固化组合物、固化体及其制造方法 - Google Patents
可光致固化组合物、固化体及其制造方法 Download PDFInfo
- Publication number
- CN1225489C CN1225489C CNB018102506A CN01810250A CN1225489C CN 1225489 C CN1225489 C CN 1225489C CN B018102506 A CNB018102506 A CN B018102506A CN 01810250 A CN01810250 A CN 01810250A CN 1225489 C CN1225489 C CN 1225489C
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- Prior art keywords
- expression
- composition
- methyl
- compound
- acrylate
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- 238000000034 method Methods 0.000 title claims description 39
- 230000008569 process Effects 0.000 title description 3
- 239000000203 mixture Substances 0.000 claims abstract description 204
- -1 mercapto compound Chemical class 0.000 claims abstract description 162
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 17
- 239000004615 ingredient Substances 0.000 claims abstract description 8
- 150000001875 compounds Chemical class 0.000 claims description 59
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 56
- 239000001301 oxygen Substances 0.000 claims description 31
- 229910052760 oxygen Inorganic materials 0.000 claims description 31
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 22
- 125000002723 alicyclic group Chemical group 0.000 claims description 22
- 238000004519 manufacturing process Methods 0.000 claims description 22
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- 238000007334 copolymerization reaction Methods 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 12
- 239000004973 liquid crystal related substance Substances 0.000 claims description 11
- 125000001118 alkylidene group Chemical group 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 10
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 239000007870 radical polymerization initiator Substances 0.000 claims description 8
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 229940125904 compound 1 Drugs 0.000 claims description 5
- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical compound [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract description 45
- 230000001976 improved effect Effects 0.000 abstract description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 12
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- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 6
- 239000012948 isocyanate Substances 0.000 description 6
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- 229910001507 metal halide Inorganic materials 0.000 description 6
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- 238000002156 mixing Methods 0.000 description 6
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 6
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 6
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- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 4
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- QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- CMQUQOHNANGDOR-UHFFFAOYSA-N 2,3-dibromo-4-(2,4-dibromo-5-hydroxyphenyl)phenol Chemical compound BrC1=C(Br)C(O)=CC=C1C1=CC(O)=C(Br)C=C1Br CMQUQOHNANGDOR-UHFFFAOYSA-N 0.000 description 3
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical group OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 3
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- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 3
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- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 3
- PODOEQVNFJSWIK-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethoxyphenyl)methanone Chemical compound COC1=CC(OC)=CC(OC)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 PODOEQVNFJSWIK-UHFFFAOYSA-N 0.000 description 3
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- BZJTUOGZUKFLQT-UHFFFAOYSA-N 1,3,5,7-tetramethylcyclooctane Chemical group CC1CC(C)CC(C)CC(C)C1 BZJTUOGZUKFLQT-UHFFFAOYSA-N 0.000 description 2
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- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 2
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- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 2
- NMPNTBQOLRXPGK-UHFFFAOYSA-N phenyl-(4-phenylmethoxyphenyl)methanone Chemical class C=1C=C(OCC=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 NMPNTBQOLRXPGK-UHFFFAOYSA-N 0.000 description 2
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- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
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- WKMKTIVRRLOHAJ-UHFFFAOYSA-N oxygen(2-);thallium(1+) Chemical compound [O-2].[Tl+].[Tl+] WKMKTIVRRLOHAJ-UHFFFAOYSA-N 0.000 description 1
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- LYKRPDCJKSXAHS-UHFFFAOYSA-N phenyl-(2,3,4,5-tetrahydroxyphenyl)methanone Chemical compound OC1=C(O)C(O)=CC(C(=O)C=2C=CC=CC=2)=C1O LYKRPDCJKSXAHS-UHFFFAOYSA-N 0.000 description 1
- LYXOWKPVTCPORE-UHFFFAOYSA-N phenyl-(4-phenylphenyl)methanone Chemical compound C=1C=C(C=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 LYXOWKPVTCPORE-UHFFFAOYSA-N 0.000 description 1
- AKWGDOVKFBLLNJ-UHFFFAOYSA-N phenyl-(6-sulfinylcyclohexa-2,4-dien-1-yl)methanone Chemical compound S(=O)=C1C(C(=O)C2=CC=CC=C2)C=CC=C1 AKWGDOVKFBLLNJ-UHFFFAOYSA-N 0.000 description 1
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 1
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- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- AZIQALWHRUQPHV-UHFFFAOYSA-N prop-2-eneperoxoic acid Chemical compound OOC(=O)C=C AZIQALWHRUQPHV-UHFFFAOYSA-N 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
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- 230000009467 reduction Effects 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
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- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910000108 silver(I,III) oxide Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910003438 thallium oxide Inorganic materials 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 230000035922 thirst Effects 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 229910021654 trace metal Inorganic materials 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
- G03F7/0275—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with dithiol or polysulfide compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F22/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
- C08F22/10—Esters
- C08F22/1006—Esters of polyhydric alcohols or polyhydric phenols, e.g. ethylene glycol dimethacrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/20—Esters of polyhydric alcohols or phenols, e.g. 2-hydroxyethyl (meth)acrylate or glycerol mono-(meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/30—Esters containing oxygen in addition to the carboxy oxygen containing aromatic rings in the alcohol moiety
- C08F220/301—Esters containing oxygen in addition to the carboxy oxygen containing aromatic rings in the alcohol moiety and one oxygen in the alcohol moiety
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/10—Esters
- C08F222/1006—Esters of polyhydric alcohols or polyhydric phenols
- C08F222/102—Esters of polyhydric alcohols or polyhydric phenols of dialcohols, e.g. ethylene glycol di(meth)acrylate or 1,4-butanediol dimethacrylate
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- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/0005—Production of optical devices or components in so far as characterised by the lithographic processes or materials used therefor
- G03F7/0007—Filters, e.g. additive colour filters; Components for display devices
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
- C09K2323/06—Substrate layer characterised by chemical composition
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- Spectroscopy & Molecular Physics (AREA)
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- Crystallography & Structural Chemistry (AREA)
- Optics & Photonics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
双(甲基)丙烯酸酯 | 单(甲基)丙烯酸酯 | 巯基化合物 | |
实施例1 | (A)94 | (B)6 | (C)6 |
实施例2 | (A)92 | (B)8 | (C)6 |
实施例3 | (A)96 | (B)4 | (C)6 |
比较例1 | (A)99.5 | (B)0.5 | (C)6 |
比较例2 | (A)60 | (B)40 | (C)6 |
比较例3 | (A)94 | (B)6 | 无 |
光线透射率(%) | 双折射(nm) | 耐热性Tg(℃) | 耐冲击性(cm) | 挠曲弹性模量(MPa) | 吸水率(%) | 脱膜性 | |
实施例1 | 92 | 0.4 | 190 | 100 | 4000 | 0.5 | ○ |
实施例2 | 92 | 0.4 | 190 | 110 | 4100 | 0.5 | ○ |
实施例3 | 92 | 0.4 | 190 | 90 | 3900 | 0.5 | ○ |
比较例1 | 92 | 1.0 | 190 | 60 | 3700 | 0.5 | △ |
比较例2 | 92 | 0.4 | 130 | 100 | 3000 | 1.0 | ○ |
比较例3 | 91 | 5.0 | 250 | 40 | 3400 | 0.3 | × |
光线透射率(%) | 双折射(nm) | 耐热性Tg(℃) | 耐冲击性(cm) | 挠曲弹性模量(MPa) | 吸水率(%) | 脱模性 | 紫外线照射试验时色相(YI值) | ||
试验前 | 试验后 | ||||||||
实施例4 | 91 | 0.6 | 190 | 75 | 4100 | 0.5 | ○ | 1.46 | 1.78 |
实施例5 | 91 | 0.6 | 190 | 65 | 3900 | 0.5 | ○ | 1.49 | 1.86 |
实施例6 | 92 | 0.5 | 190 | 65 | 3800 | 0.5 | ○ | 1.39 | 1.95 |
实施例7 | 91 | 0.6 | 190 | 70 | 4000 | 0.5 | ○ | 1.55 | 4.15 |
实施例8 | 92 | 0.7 | 190 | 65 | 3900 | 0.5 | ○ | 1.63 | 3.73 |
实施例9 | 91 | 5.5 | 190 | 70 | 4100 | 0.5 | ○ | 1.56 | 3.59 |
光线透射率(%) | 双折射(nm) | 耐热性Tg(℃) | 耐冲击性(cm) | 挠曲弹性模量(MPa) | 吸水率(%) | 脱模性 | 加热时色相(YI值) | ||
试验前 | 试验后 | ||||||||
实施例10 | 92 | 0.6 | 190 | 70 | 4000 | 0.5 | ○ | 0.76 | 1.74 |
实施例11 | 91 | 0.5 | 190 | 70 | 3900 | 0.5 | ○ | 0.89 | 1.96 |
实施例12 | 92 | 0.5 | 190 | 65 | 4000 | 0.5 | ○ | 0.95 | 1.99 |
实施例13 | 92 | 0.6 | 190 | 70 | 4000 | 0.5 | ○ | 1.32 | 3.03 |
实施例14 | 91 | 5.5 | 190 | 65 | 4100 | 0.5 | ○ | 1.29 | 2.95 |
Claims (13)
Applications Claiming Priority (12)
Application Number | Priority Date | Filing Date | Title |
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JP94717/00 | 2000-03-30 | ||
JP2000094717 | 2000-03-30 | ||
JP94716/2000 | 2000-03-30 | ||
JP94716/00 | 2000-03-30 | ||
JP94717/2000 | 2000-03-30 | ||
JP2000094716 | 2000-03-30 | ||
JP336117/2000 | 2000-11-02 | ||
JP2000336117 | 2000-11-02 | ||
JP336118/2000 | 2000-11-02 | ||
JP336117/00 | 2000-11-02 | ||
JP336118/00 | 2000-11-02 | ||
JP2000336118 | 2000-11-02 |
Publications (2)
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CN1432029A CN1432029A (zh) | 2003-07-23 |
CN1225489C true CN1225489C (zh) | 2005-11-02 |
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US (1) | US6759104B2 (zh) |
EP (1) | EP1275668B1 (zh) |
KR (1) | KR100795740B1 (zh) |
CN (1) | CN1225489C (zh) |
AU (1) | AU2001242817A1 (zh) |
WO (1) | WO2001074918A1 (zh) |
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JP2004198542A (ja) * | 2002-12-16 | 2004-07-15 | Showa Denko Kk | カラーフィルターブラックマトリックスレジスト組成物及びその組成物に用いる感光性組成物 |
KR20060024375A (ko) * | 2003-05-26 | 2006-03-16 | 오므론 가부시키가이샤 | 경화형 수지 조성물, 광학 부품 및 광도파로 |
US8097399B2 (en) * | 2004-03-22 | 2012-01-17 | 3D Systems, Inc. | Photocurable compositions |
US8105759B2 (en) * | 2005-07-05 | 2012-01-31 | Hitachi Chemical Company, Ltd. | Photosensitive resin composition, and, photosensitive element, method for forming resist pattern, method for manufacturing printed wiring board and method for manufacturing partition wall for plasma display panel using the composition |
JP2007234424A (ja) | 2006-03-01 | 2007-09-13 | Nitto Denko Corp | 透明導電性フィルムおよびタッチパネル |
KR20090057292A (ko) * | 2006-08-31 | 2009-06-04 | 내셔날 인스티튜트 오브 어드밴스드 인더스트리얼 사이언스 앤드 테크놀로지 | 태양 전지용 투명 전극 기판 |
US20080095995A1 (en) * | 2006-10-18 | 2008-04-24 | Hong Rae Cha | Filter and flat panel display device using the filter |
CN105669900A (zh) * | 2008-12-09 | 2016-06-15 | 出光兴产株式会社 | 光学部件用树脂原料组合物、光学部件用树脂和光学部件 |
US7766668B1 (en) * | 2009-02-11 | 2010-08-03 | Avx Corporation | Low profile electrical conductor assembly for interconnecting conductive components in a stacked configuration |
US8530119B2 (en) | 2009-05-20 | 2013-09-10 | Sumitomo Bakelite Co., Ltd. | Positive photosensitive resin composition, cured film, protective film, interlayer insulating film, and semiconductor device and display element using the same |
TWI381303B (zh) | 2010-02-09 | 2013-01-01 | Oji Paper Co | 導電性積層體及使用其之觸控面板 |
JP5869916B2 (ja) * | 2012-03-02 | 2016-02-24 | デンカ株式会社 | 光硬化性樹脂組成物 |
EP2828311A1 (de) | 2012-03-19 | 2015-01-28 | Basf Se | Strahlungshärtbare wässrige dispersionen |
US9193888B2 (en) | 2012-03-19 | 2015-11-24 | Basf Se | Radiation-curable aqueous dispersions |
KR101611006B1 (ko) * | 2013-08-13 | 2016-04-08 | 제일모직주식회사 | 광경화 조성물 및 이를 사용하여 제조된 봉지화된 장치 |
AU2014345787B2 (en) | 2013-11-05 | 2017-10-26 | Sika Technology Ag | Novel binding agent systems |
US10577471B2 (en) | 2014-10-01 | 2020-03-03 | Basf Se | Method for curing curable compositions |
CN112707984B (zh) * | 2021-01-11 | 2022-04-05 | 西安交通大学 | 一种基于动态共价键的4d打印光敏树脂及其制备方法 |
US11753497B2 (en) * | 2021-04-29 | 2023-09-12 | Canon Kabushiki Kaisha | Photocurable composition |
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GB9211731D0 (en) * | 1992-06-03 | 1992-07-15 | Merck Patent Gmbh | Electrooptical liquid crystal system |
JPH061869A (ja) * | 1992-06-22 | 1994-01-11 | Idemitsu Petrochem Co Ltd | ホスファゼン系樹脂被覆部材 |
KR960012438B1 (ko) * | 1993-07-10 | 1996-09-20 | 주식회사 코오롱 | 농업용 폴리에스테르 필름 |
JPH08240819A (ja) * | 1995-03-01 | 1996-09-17 | Fuji Xerox Co Ltd | 液晶表示素子及びその駆動方法 |
JP3780554B2 (ja) * | 1995-03-15 | 2006-05-31 | 大日本インキ化学工業株式会社 | 活性エネルギー線硬化型樹脂組成物、液晶デバイス及びその製造法 |
CN1115352C (zh) * | 1995-05-30 | 2003-07-23 | 索拉国际控股有限公司 | 高折射率/高阿贝数组合物 |
JPH09152510A (ja) | 1995-09-25 | 1997-06-10 | Mitsubishi Chem Corp | 低複屈折光学部材及びその製造方法 |
JP3662666B2 (ja) * | 1996-04-18 | 2005-06-22 | 日本ペイント株式会社 | 紫外線硬化型液状組成物及び塗膜形成方法 |
JPH1025624A (ja) | 1996-07-08 | 1998-01-27 | Mitsubishi Chem Corp | 炭素繊維及び炭素繊維集合体 |
JP3592842B2 (ja) | 1996-07-08 | 2004-11-24 | 帝人ファイバー株式会社 | ポリエステル系弾性繊維及びそれからなる伸縮性湿式不織布 |
JP3540115B2 (ja) | 1996-07-09 | 2004-07-07 | 三菱化学株式会社 | 樹脂組成物及びこれを活性エネルギー線により硬化させてなる部材 |
JPH10231340A (ja) * | 1996-12-20 | 1998-09-02 | Takeda Chem Ind Ltd | 光硬化性樹脂組成物およびその製造方法 |
US6075065A (en) | 1996-12-20 | 2000-06-13 | Takeda Chemical Industries, Ltd. | Photocurable resin composition and a method for producing the same |
JP3901821B2 (ja) * | 1998-02-06 | 2007-04-04 | 三菱化学株式会社 | 低複屈折光学部材、その成形用樹脂組成物及び光学部材の製造方法 |
EP1112995B1 (en) * | 1998-09-11 | 2007-04-11 | Nissan Chemical Industries, Ltd. | Alicyclic compounds and curable resin composition |
-
2001
- 2001-03-27 AU AU2001242817A patent/AU2001242817A1/en not_active Abandoned
- 2001-03-27 KR KR1020027012869A patent/KR100795740B1/ko active IP Right Grant
- 2001-03-27 CN CNB018102506A patent/CN1225489C/zh not_active Expired - Lifetime
- 2001-03-27 WO PCT/JP2001/002490 patent/WO2001074918A1/ja active Application Filing
- 2001-03-27 EP EP01915848A patent/EP1275668B1/en not_active Expired - Lifetime
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2002
- 2002-09-30 US US10/259,778 patent/US6759104B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
KR100795740B1 (ko) | 2008-01-17 |
CN1432029A (zh) | 2003-07-23 |
EP1275668B1 (en) | 2011-05-11 |
WO2001074918A1 (fr) | 2001-10-11 |
EP1275668A1 (en) | 2003-01-15 |
US6759104B2 (en) | 2004-07-06 |
AU2001242817A1 (en) | 2001-10-15 |
US20030118941A1 (en) | 2003-06-26 |
EP1275668A4 (en) | 2009-06-17 |
KR20020087436A (ko) | 2002-11-22 |
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